Porous polymer coatings

ABSTRACT

The present invention provides porous polymer coatings having adhesive and air flow resistive properties. The porous polymer coating comprises a polymeric foam having a void fraction of greater than about 15% and an air permeability greater than 3 cubic feet per minute per square foot as measured based on ASTM D737-04.

RELATED APPLICATIONS

This application is a continuation application of U.S. patentapplication Ser. No. 14/528,061, filed Oct. 30, 2014, which claimspriority from U.S. Provisional Application Ser. No. 61/897,969, filedOct. 31, 2013, the disclosure of each of which is hereby incorporated byreference herein in their entirety.

FIELD OF THE INVENTION

The present application relates to porous polymer coatings.

BACKGROUND

Acoustically effective materials are used in a variety of applicationsand products, including, but not limited to, transportationapplications, building applications, architectural applications,automobiles, heavy equipment, bus, rail transport vehicles, aircraft,air ducts, appliances, baffles, ceiling tiles and office partitions.

An acoustically effective facing may be applied to a substrate to impartand/or adjust one or more acoustic properties of the substrate.Exemplary acoustic facings are described in U.S. Patent Publication Nos.2010/0147621 and 2013/0186706 and U.S. Pat. Nos. 8,403,108, 8,439,161,and 8,607,929; the disclosure of each of which is incorporated herein byreference in its entirety.

Acoustically effective facings may comprise an adhesive (e.g., athermally activated adhesive). For example, some acoustically effectivefacings have an adhesive on one side thereof to allow for bonding to athicker acoustic absorbing layer. Adhesive may be applied toacoustically effective facings by various means, including, but notlimited to, screen printing, gravure coating, foam coating, die coatingand scatter coating.

SUMMARY OF THE INVENTION

The present application provides a porous polymer coating. Such porouspolymeric coatings imparts useful adhesive and acoustic properties to asubstrate. Furthermore, we have discovered that the acoustic propertiesof such a composite material may be modulated by controlling the passageof air by the porous polymeric coating (e.g., by modulating the porosityof the porous polymeric coating). The porous polymer coating comprises apolymeric foam having a void fraction of greater than about 15% and anair permeability greater than 3 cubic feet per minute per square foot asmeasured based on ASTM D737-04.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an image of the surface of a porous polymer coating accordingto some embodiments of the present invention. The image was acquiredusing a scanning electron microscope.

FIG. 2 is a cross-sectional image of the porous polymer coating depictedin FIG. 1. The image was acquired using a scanning electron microscope.

FIG. 3 is an image of the surface of a porous polymer coating accordingto some embodiments of the present invention. The sample was compressedprior to imaging. The image was acquired using a scanning electronmicroscope.

FIG. 4 is a cross-sectional image of the porous polymer coating depictedin FIG. 3. The image was acquired using a scanning electron microscope.

FIG. 5 is an image of the surface of a porous polymer coating accordingto some embodiments of the present invention. The sample was molded toand then removed from a web of fiberglass fibers prior to imaging.Residual glass fibers can be seen on the surface of the porous polymercoating. The image was acquired using a scanning electron microscope.

FIG. 6 is a cross-sectional image of the porous polymer coating depictedin FIG. 5. The image was acquired using a scanning electron microscope.

FIG. 7 is an image of the surface of a porous polymer coating accordingto some embodiments of the present invention. The image was acquiredusing a scanning electron microscope.

FIG. 8 is an image of the surface of a porous polymer coating accordingto some embodiments of the present invention. The image was acquiredusing a scanning electron microscope.

FIG. 9 is a graph comparing the air permeabilities of compositematerials according to some embodiments of the present inventiondemonstrating that for a given formulation, fabric, and applicationsystem, the air permeability can be varied by varying the coatingweight.

FIG. 10 is a graph similar to FIG. 9 comparing the air permeabilities ofcomposite materials according to some embodiments of the presentinvention demonstrating that for a given formulation, fabric, andapplication system, the air permeability can be varied by varying thecoating weight, such as by varying the foam applicator gap.

FIG. 11 is a graph showing variations of coating air permeability versusdry add-on weight resulting from compound formulation changes.

FIG. 12 is a graph comparing the dry add-on weights of porous polymercoatings in composite materials according to some embodiments of thepresent invention with the coating gaps used to form those compositematerials.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is explained in greater detail below. Thisdescription is not intended to be a detailed catalog of all thedifferent ways in which the invention may be implemented or of all thefeatures that may be added to the instant invention. For example,features illustrated with respect to one embodiment may be incorporatedinto other embodiments, and features illustrated with respect to aparticular embodiment may be deleted from that embodiment. In addition,numerous variations and additions to the various embodiments suggestedherein, which do not depart from the instant invention, will be apparentto those skilled in the art in light of the instant disclosure. Hence,the following specification is intended to illustrate some particularembodiments of the invention, and not to exhaustively specify allpermutations, combinations and variations thereof.

It will be understood that when an element or layer is referred to asbeing “on”, “attached to”, “connected to”, “coupled to”, “coupled with”or “contacting” another element or layer, it can be directly on,connected or coupled to the other element or layer or interveningelements or layers may be present. In contrast, when an element isreferred to as being “directly on,” “directly connected to” or “directlycoupled to” another element or layer, there are no intervening elementsor layers present. It will be appreciated by those of skill in the artthat a structure referred to as being “directly on,” “directly connectedto, or “directly coupled to” another structure may partially orcompletely cover one or more surfaces of the other structure. It willalso be appreciated by those of skill in the art that references to astructure or feature that is disposed “adjacent” another structure orfeature may have portions that overlap or underlie the adjacentstructure or feature.

The terminology used herein is for the purpose of describing particularembodiments only and is not intended to be limiting of the invention.

Unless otherwise defined, all terms (including technical and scientificterms) used herein have the same meaning as commonly understood by oneof ordinary skill in the art to which this invention belongs. It will befurther understood that terms, such as those defined in commonly useddictionaries, should be interpreted as having a meaning that isconsistent with their meaning in the context of the specification andrelevant art and should not be interpreted in an idealized or overlyformal sense unless expressly so defined herein. Well-known functions orconstructions may not be described in detail for brevity and/or clarity.

As used herein, the singular forms “a”, “an” and “the” are intended toinclude the plural forms as well, unless the context clearly indicatesotherwise.

As used herein, the term “about,” when used in reference to a measurablevalue such as an amount of mass, dose, time, temperature, and the like,is meant to encompass variations of 20%, 10%, 5%, 1%, 0.5%, or even 0.1%of the specified amount.

As used herein, “ASTM” refers to ASTM, International, 100 Barr HarborDrive, P.O. Box C700, West Conschoken, Pa. 19428-2959 USA.

As used herein, the term “air permeability” refers to the rate of airflow passing perpendicularly through a known area of a material under aprescribed air pressure differential. See, e.g., ASTM Standard D737-04,“Standard Test Method for Air Permeability of Textile Fabrics,” ASTMInternational (2012) of 0.5 inches of water column pressure drop. Unlessotherwise specified, the air permeability measurements described hereinare expressed in cubic feet per minute per square foot (hereinafter“cfm”).

As used herein, the term “airflow resistance” refers to the impedence ofairflow through a known area of a material under a prescribed airpressure differential. See, e.g., ASTM Standard C522-03, “Standard TestMethod for Airflow Resistance of Acoustical Materials,” ASTMInternational (2009). Unless otherwise specified, the airflow resistancemeasurements described herein were measured based on ASTM StandardC522-03, “Standard Test Method for Airflow Resistance of AcousticalMaterials,” ASTM International (2009). Unless otherwise specified, theair permeability measurements described herein are expressed in Rayls.Air permeability and airflow resistance are reflective of expectedacoustic impedance.

As used herein, the term “and/or” includes any and all combinations ofone or more of the associated listed items.

As used herein, the term “batt” refers to a sheet or web of unbounded orlightly bonded fibers.

As used herein, the term “blow ratio” refers to the ratio of air toliquid in a porous material (e.g., a foam). For example, if a knownvolume of liquid was a weight of 20 grams, and air is introduced intothe liquid such that an equal volume of the foamed liquid has a weightof 2 grams, the blow ratio of the foamed liquid is 10 (i.e., the foamedliquid has an air to liquid ratio of 10:1).

As used herein, the terms “comprise,” “comprises,” “comprising,”“include,” “includes” and “including” specify the presence of statedfeatures, integers, steps, operations, elements, and/or components, butdo not preclude the presence or addition of one or more other features,integers, steps, operations, elements, components, and/or groupsthereof.

As used herein, the term “consists essentially of” (and grammaticalvariants thereof), as applied to the compositions and methods of thepresent invention, means that the compositions/methods may containadditional components so long as the additional components do notmaterially alter the composition/method. The term “materially alter,” asapplied to a composition/method, refers to an increase or decrease inthe effectiveness of the composition/method of greater than about 20% ormore. For example, a component added to a composition of the presentinvention would “materially alter” the composition if it increases ordecreases the composition's durability by greater than 20%.

As used herein, the terms “increase” and “enhance” (and grammaticalvariants thereof) refer to an increase in the specified parameter ofgreater than about 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%,40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%,150%, 175%, 200%, 250%, 300% or more.

As used herein, the terms “inhibit”, “decrease,” and “reduce” (andgrammatical variants thereof) refer to a decrease in the specifiedparameter of greater than about 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%,30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%,99% or more.

As used herein, the term “latex” refers to an aqueousdispersion/emulsion of one or more polymers.

As used herein, the term “porous polymer coating” refers to a porous,polymeric structure that controls the passage of air.

As used herein, the term “Rayl” refers to specific acoustic impedanceand/or characteristic acoustic impedance of an article. As one skilledin the art will readily appreciate, the acoustic impedance may bedefined as one or two units: an MKS unit and a CGS unit. In MKS units, 1Rayl equals 1 pascal-second per meter (Pa·s·m⁻¹). In CGS unites, 1 Raylequals 1 dyne-second per cubic centimeter (dyn·s·cm⁻³). 1 CGS Rayl=10MKS Rayls. Unless otherwise specified, the Rayls measurements describedherein are expressed in MKS units.

As used herein, the term “reticulated foam” refers to a foam wherein themajority of the bubbles/cells are not fully intact. In some embodiments,about 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 45%, 50%, 55% 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100% of the bubbles/cellswithin the reticulated foam are open bubbles/cells. In some embodiments,the bubbles/cells are open to the extent that only the common/sharedboundaries of the bubbles/cells remain intact.

As used herein, the term “thermally activatable” refers to a materialthat adhesively bonds when heated.

All publications, patent applications, patents, and other referencesmentioned herein are incorporated by reference in their entirety.

Porous polymer coatings of the present invention may comprise anysuitable polymer, including, but not limited to, thermoplastic polymersand non-thermoplastic polymers. In some embodiments, porous polymercoatings of the present invention comprise, consist essentially of orconsist of one or more thermoplastic polymers and/or one or morenon-thermoplastic polymers. In some embodiments, porous polymer coatingsof the present invention comprise, consist essentially of or consist ofone or more thermoset polymers. In some embodiments, porous polymercoatings of the present invention comprise, consist essentially of orconsist of one or more water soluble polymers. In some embodiments,porous polymer coatings of the present invention comprise, consistessentially of or consist of one or more polymers derived from anemulsion or a dispersion (e.g., one or more polymer layers derived froman emulsion or dispersion). In some embodiments, porous polymer coatingsof the present invention comprise, consist essentially of or consist ofone or more melted and extruded polymers. In some embodiments, porouspolymer coatings of the present invention comprise, consist essentiallyof or consist of one or more copolymers and/or one or more polymerblends. In some embodiments, porous polymer coatings of the presentinvention comprise, consist essentially of or consist of one or morelatex binders.

Porous polymer coatings of the present invention may comprise anysuitable thermoplastic polymer, including, but not limited to,polyacrylates, polyvinylacetates, styrene butadiene rubbers,diallylorthophthalates, ionomers, formulated epoxys, polysulfones,perfluorinated polymers and elastomers, polyether-etherketones,acrylonitrilebutadienstyrenes, polycarbonates, vinylesters, styrenecopolymers, polyamides, polyamines, ethylenevinylacetates,polyvinyalcohols, polyvinylchlorides, polyvinylidiene chloride,chlorinated polyethylenes, polyesters, nitriles, polyurethanes,polyethylenes, polypropylenes. In some embodiments, porous polymercoatings of the present invention comprise, consist essentially of orconsist of one or more thermoplastic copolymers and/or one or morethermoplastic polymer blends. In some embodiments, the porous polymercoatings of the present invention comprise one or more acrylicthermoplastic polymers and one or more copolyester thermoset polymers.

Porous polymer coatings of the present invention may comprise anysuitable additive, including, but not limited to, porogenic agents,adhesive agents, blowing agents, foaming agents, stabilizing agents(e.g., foam stabilizers, thermal stabilizers, light stabilizers, etc.),lubricating agents, tackifying agents, slip agents, elastic agents,antistatic agents, electrically conductive agents, antimicrobial agents(e.g., antibacterial agents, mildewcides, etc.), antifungal agents,coloring agents (e.g., pigments), repellant agents (e.g., waterrepellants, alcohol repellants, oil repellants, soil repellants, stainrepellants, etc), flame retardant agents, UV resistant agents, UVabsorption agents and filler agents, such as clay, calcium carbonate,minerals, polymer or mineral (e.g., glass) beads, metallic fillers, andthe like. In some embodiments, porous polymer coatings of the presentinvention comprise one or more active agents. In some embodiments,porous polymer coatings of the present invention comprise one or moreagents that increase the durability of the porous polymer coating(and/or a substrate to which the porous polymer coating is applied). Forexample, the porous polymer coating may comprise one or more isocyanates(e.g., blocked ioscyanates). In some embodiments, porous polymercoatings of the present invention comprise one or more flame retardantchemistries or additives. For example, the porous polymer coating maycomprise one or more flame retardant antimony compounds (e.g., antimonyoxides), one or more flame retardant boron compounds (e.g., ammoniumborate, borax, boric acid, ethanolammonium borate and/or zinc borate),one or more flame retardant halogen compounds (e.g., ammonium bromide,ammonium chloride, brominated/chlorinated binders,brominated/chlorinated additives and/or brominated/chlorinatedparaffin), one or more flame retardant nitrogen compounds (e.g.,monoammonium phosphate, diammonium phosphate, ammonium borate, ammoniumbromide, ammonium chloride, ammonium polyphosphate, melamine, and/orurea), organic and inorganic containing compounds, phosphorouscontaining compounds (e.g. ammonium polyphosphate), and/or one or moreflame retardant sulfur compounds (e.g., ammonium sulfamate). In someembodiments, porous polymer coatings of the present invention compriseone or more antistats. For example, the porous polymer coating maycomprise one or more salts, sodium chloride, sodium nitrate, sodiumsulfate, or phosphate esters and/or one or more quaternary ammoniumcompounds.

Exemplary porous polymer coatings are described below in Table 1. Theair permeability and airflow resistance of the porous polymer coatingscan be modulated by adjusting porosity thereof (e.g., by adjusting theblow ratio, drying conditions and/or chemical additives used duringformation).

TABLE 1 Exemplary Porous Polymer Coatings Formula 1 Formula 2 Formula 3Formula 4 Ingredient Description (grams) (grams) (grams) (grams) WaterCarrier medium 75 160 Binder Polymer dispersion or 196 emulsion FlovanCGN Phosphate based 70 40 flame retardant Exolit 462 Phase 2 APP 24encapsulated with melamine Unifroth 144 Anionic foaming 2.5 agentStanfax 320 Ammonium stearate 2.5 6 12 12 Synthebond Styrene acrylate200 154 90 SA 110 copolymer dispersion Fuller PN- Styrene acrylate 1003691-M copolymer emulsion Synthebond Styrene acrylate 154 90 SA103copolymer dispersion Ammonyx LO Lauramine oxide 6 8 8 Aqueous Base forpH 2 2 Ammonium adjustment Hydroxide

Porous polymer coatings of the present invention may be formed using anysuitable method/composition/apparatus for introducing air into a polymerdispersion or emulsion, including, but not limited to, blowing agents,foaming agents, volatile liquids, commercial mixers (e.g., Hobart®(Troy, Ohio) mixers, KitchenAid® (St. Joseph, Mich.) mixers, etc.) andcommercial foam generator systems (e.g., the CFS® System by GastonSystems, Inc. of Stanley, N.C.). As will be appreciated by one skilledin the art, the porosity and/or consistency of the porous polymercoating may be selectively adjusted (i.e., tuned) by changing theconstituents of the porous polymer coating and/or thetool/attachment/settings used to mix the polymer dispersion. Forexample, the porosity and/or consistency of a porous polymer coating maybe selectively adjusted by changing the speed at which the polymerdispersion is mixed and/or the attachment with which the polymerdispersion is mixed.

Porous polymer coatings of the present invention may have any suitablebasis weight. In some embodiments, the porous polymer coating has abasis weight of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 25,40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 grams per squaremeter (gsm) or less. In some embodiments, the porous polymer coating hasa basis weight of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30,25, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 gsm or more. Insome embodiments, a porous polymer coatings of the present invention isapplied to a substrate (e.g., a fabric) that has a basis weight of about10 to about 100 gsm.

Porous polymer coatings of the present invention may have an airflowresistance of about 100, 125, 150, 175, 200, 225, 250, 300, 350, 400,450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100,1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500, 1600, 1700, 1800, 1900,2000, 2100, 2200, 2300, 2400, 2500, 2600, 2700, 2800, 2900, 3000, 3200,3400, 3600, 3800, 4000, 4200, 4400, 4600, 4800, 5000, 5500, 6000, 6500,7000, 7500, 8000, 8500, 9000, 9500, 10000 Rayls or more when testedbased on ASTM Standard C522-03, “Standard Test Method for AirflowResistance of Acoustical Materials,” ASTM International (2009). In someembodiments, the porous polymer coating has an airflow resistance ofbetween about 100 and about 10,000 Rayls.

Porous polymer coatings of the present invention may have an airpermeability of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15,16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85,90, 95, 100, 110, 120, 130, 140, 150 cfm or less. In some embodiments,the porous polymer coating has an air permeability of between about 10and about 100 cfm.

Porous polymer coatings of the present invention may have any suitableporous structure, including, but not limited to, reticulated porousstructures and intact porous structures. In some embodiments, the porouspolymer coating comprises a low density, reticulated foam structure. Insome embodiments, the porous polymer coating comprises a reticulatedfoam structure formed by drying an intact foam structure such thatintact bubbles/cells are converted to open bubbles/cells In someembodiments, the porous polymer coating has a void fraction of about 5%,10%, 15%, 20%, 35%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 71%,72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%,86%, 87%, 88%, 89% 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% ormore.

Porous polymer coatings of the present invention may retain their porousstructure following compression (as shown in FIGS. 3-4) and/or moldingto a substrate (as shown in FIGS. 5-6). In some embodiments, the voidfraction of the porous polymer coating is reduced by about 1%, 2%, 3%,4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%,55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or less following heatactivation and molding/bonding to one or more substrates. In someembodiments, the void fraction of the porous polymer coating is reducedby about 10%, about 25%, about 50% or about 75% following heatactivation and molding/bonding to one or more substrates.

Porous polymer coatings of the present invention may have any suitableblow ratio. In some embodiments, the porous polymer coating has a blowratio of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16,17, 18, 19, 20 or more. In some embodiments, the porous polymer coatinghas a blow ratio of between about 1 and about 10.

Porous polymer coatings of the present invention may be applied to oneor more substrates to form a composite material. In some embodiments,the composite material comprises a porous polymer coating of the presentinvention interposed between two substrates Porous polymer coatings ofthe present invention may be applied to any suitable substrate,including, but not limited to, batts, fabrics, nets, papers and films.In some embodiments, porous polymer coatings of the present inventionare applied to building materials. In some embodiments, porous polymercoatings of the present invention are applied to nonporous substrates,such as a release liner, and then removed from the substrate for usewithout a substrate.

Porous polymer coatings of the present invention may be applied to anysuitable batt, including, but not limited to, homopolymer batts,multifiber batts (e.g., shoddy batts), felts (e.g., needled felts),vertically lapped batts, pleated batts and thermally bonded batts. Insome embodiments, porous polymer coatings are applied to battscomprising one or more glass fibers (e.g., glass insulation).

Porous polymer coatings of the present invention may be applied to anysuitable type of fabric, including, but not limited to, woven fabrics,nonwoven fabrics and knit fabrics.

Porous polymer coatings of the present invention may be applied to anysuitable nonwoven fabric, including, but not limited to, spunlacedfabrics, spunbonded fabrics, needlepunched fabrics, stitchbondedfabrics, thermal bonded fabrics, powder bonded fabrics, chemical bondedfabrics, wet laid fabrics and air laid fabrics. In some preferredembodiments, the porous polymer coating is applied to a spunlacedfabric.

Porous polymer coatings of the present invention may be applied tofabrics that have undergone any suitable mechanical treatment,including, but not limited to, calendaring, creping, embossing, ringrolling and stretching. In some embodiments of the invention the porouscoating is applied to a substrate that has been chemically treated forcertain properties that include, flame retardancy, oil, alcohol or waterrepellency, antistat, antimicrobial, corrosion inhibition, color,binders, and the like.

Porous polymer coatings of the present invention may be applied tofabrics having any suitable three-dimensional pattern(s). In someembodiments, porous polymer coatings of the present invention areapplied to a nonwoven fabric comprising a three-dimensional pattern thatmimics the three-dimensional texture of a woven textile (e.g., hopsack,terrycloth or twill). In some embodiments, porous polymer coatings ofthe present invention are applied to a nonwoven fabric comprising athree-dimensional pattern such that one or more surfaces of the fabric(e.g., the face of the fabric) has an average surface roughness ofgreater than about 5, 10, 20, 30, 40, 50, 60, 70, 75, 80, 90, 100, 125,150, 175, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750,800, 850, 900, 950, 1000 or more microns (as measured based on theKawabata Evaluation System (KES) using a KES-FB4 Surface RoughnessTester and/or as measured using a profilometer, for example).

Porous polymer coatings of the present invention may be applied tosubstrates comprising any suitable fiber type, including, but notlimited to, batts/fabrics that comprise, consist essentially of orconsist of natural fibers and/or synthetic fibers. In some embodiments,porous polymer coatings of the present invention are applied tobatts/fabrics comprising, consisting essentially of or consisting ofbamboo fibers, camel hair fibers, graphite fibers, cotton fibers, flaxfibers, hemp fibers, jute fibers, polylactic acid fibers, silk fibers,sisal fibers, wood pulp and/or wool (e.g., alpaca, angora, cashmere,chiengora, guanaco, llama, mohair, pashmina, sheep and/or vicuna)fibers. In some embodiments, porous polymer coatings of the presentinvention are applied to batts/fabrics comprising, consistingessentially of or consisting of acrylic fibers, carbon fibers,fluorocarbon fibers, glass fibers (e.g., melt blown glass fibers,spunbonded glass fibers, air laid glass fibers and wet laid glassfibers), lyocell fibers, melamine fibers, modacrylic fibers,polyacrylonitrile (e.g., oxidized polyacrylonitrile) fibers, polyamide(e.g., nylon and/or aramid) fibers, polybenzimidazole fibers, polyesterfibers, polyimide fibers, polylactic acid fibers, polyolefin (e.g.,polyethylene and/or polypropylene) fibers, polyphenylene benzobisoxazolefibers, polyphenylene sulfide fibers, polyvinyl acetate fibers,polyvinyl alcohol fibers, polyvinyl chloride fibers, polyvinyl fluoridefibers, polyvinylidene chloride fibers, rayon fibers, viscose fibers,modified viscose (e.g., silica-modified viscose) fibers and zylonfibers. In some embodiments, porous polymer coatings of the presentinvention are applied to batts/fabrics comprising, consistingessentially of or consisting of cellulosic fibers (e.g., bamboo fibers,cellulose acetate fibers, cellulose triacetate fibers, cotton fibers,flax fibers, hemp fibers, jute fibers, lyocell fibers, ramie fibers,sisal fibers, viscose fibers, rayon fibers, modified viscose (e.g.,silica-modified viscose) fibers and/or wood pulp). In some embodiments,porous polymer coatings of the present invention are applied tosubstrates comprising, consisting essentially of or consisting ofbicomponent fibers. For example, porous polymer coatings of the presentinvention are applied to substrates comprising, consisting essentiallyof or consisting of fibers comprising greater than two distinctconstituent monomers (e.g., polyester and polypropylene). In someembodiments, porous polymer coatings of the present invention areapplied to substrates comprising, consisting essentially of orconsisting of continuous fibers. In some embodiments, porous polymercoatings of the present invention are applied to substrates comprising ablend of fibers. (e.g. rayon and polyester). In some embodiments, porouspolymer coatings of the present invention are applied to substratescomprising staple fibers. For example, porous polymer coatings of thepresent invention are applied to batts/fabrics comprising, consistingessentially of or consisting of one or more spunbonded fibers (e.g.,flash spunbonded fibers), one or more meltblown fibers and/or one ormore spunbonded-meltblown-spunbonded composite fibers. For example, awet laid substrate such as a paper, a wet-laid nonwoven fabric, or awet-laid spunlaced fabric may be used.

Porous polymer coated substrates of the present invention may besubsequently bonded to an additional sound absorbing material to form amultilayer product that has enhanced air flow resistance and improvedsound absorbing capability. The bonding of the inventive substrate tothe additional sound absorbing material is facilitated by the adhesiveproperties of the coating. The products produced in this way includemolded sound absorbing panels for vehicles and aircraft, bonded soundabsorbing panels for architectural use, sound absorbing materials forductwork, acoustic and musical end uses such as speakers, panels forauditoriums, and the like.

Porous polymer coatings of the present invention may be applied to asubstrate having any suitable basis weight. In some embodiments, aporous polymer coatings of the present invention is applied to asubstrate (e.g., a fabric) that has a basis weight of about 10, 15, 20,25, 30, 25, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110,120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250,260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390,400, 420, 440, 460, 480, 500, 520, 540, 560, 580, 600, 650, 700, 750,800, 850, 900, 950, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700,1800, 1900 or 2000 gsm or less. In some embodiments, a porous polymercoatings of the present invention is applied to a substrate (e.g., afabric) that has a basis weight of about 10, 15, 20, 25, 30, 25, 40, 45,50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150,160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290,300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 420, 440, 460,480, 500, 520, 540, 560, 580, 600, 650, 700, 750, 800, 850, 900, 950,1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000 gsm ormore. In some embodiments, a porous polymer coatings of the presentinvention is applied to a substrate (e.g., a fabric) that has a basisweight of about 10 to about 100 gsm.

Porous polymer coatings of the present invention may be applied to asubstrate having any suitable airflow resistance. In some embodiments, aporous polymer coating of the present invention is applied to asubstrate (e.g., a fabric) that has an airflow resistance of about 1, 2,3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 125, 150,175, 200, 225, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750,800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350,1400, 1450, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300, 2400,2500 Rayls or more when tested based on ASTM Standard C522-03, “StandardTest Method for Airflow Resistance of Acoustical Materials,” ASTMInternational (2009). In some embodiments, the porous polymer coating ofthe present invention is applied to a substrate (e.g., a fabric) thathas an airflow resistance of between about 10 and about 1,000 Rayls.

Porous polymer coatings of the present invention may be applied to asubstrate having any suitable air permeability. In some embodiments, aporous polymer coating of the present invention is applied to asubstrate (e.g., a fabric) that has an air permeability of about 2, 10,15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100,110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240,250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 400, 450, 500,550, 600, 650, 700, 750, 800, 850, 900, 950, 1000 cfm or more. In someembodiments, the porous polymer coating is applied to a substrate (e.g.,a fabric) that has an air permeability of between about 10 and about1,000 cfm/sq. ft., based on ASTM Standard D737-04, ““Standard TestMethod for Air Permeability of Textile Fabrics,” ASTM International(2012).

Porous polymer coatings of the present invention may be applied to asubstrate that is a polymeric foam. Examples would be urethane foam,foamed rubber both natural and synthetic, foamed polymers such asolefins, polystyrene, acrylates, styrene butadiene, and mixtures ofpolymers.

Porous polymer coatings of the present invention may be applied to acarpet, which would enhance the sound absorption of the carpet and allowfor thermally activated bonding of the carpet to another material orsurface. Additionally, a substrate, coated with the porous coating ofthe present invention may be bonded to the back of carpet to enhance thesound absorption of the carpet in use.

Porous polymer coatings of the present invention may be applied usingany suitable method, including, but not limited to, knife coating,scrape coating, kiss coating, gap coating, foam coating, spray coating,roll coating, gravure coating, screen printing, slot coating,electrostatic coating and starved die coating. In some embodiments, theapplication process comprises greater than partially melting the porouspolymer coating. The airflow resistance of the porous polymer coatingmay remain the same (or substantially the same) following application(e.g., following the activation and adhesive bonding of the porouspolymer coating to one or more substrates). The airflow resistance ofthe porous polymer coating may change in a predictable manner followingapplication (e.g., following the activation and adhesive bonding of theporous polymer coating to one or more substrates). The porosity orpermeability of the coating or coated substrate may be further modifiedby calendaring, embossing, crushing, or chemical treatment.

Porous polymer coatings of the present invention may impart and/ormodulate any suitable characteristic to/of the substrate(s). In someembodiments, the porous polymer coating imparts one or more adhesiveproperties to and/or modulates one or more adhesive properties of thesubstrate(s). For example, the porous polymer coating may impartadhesive properties that allow two or more substrates to be moldedtogether to form a composite material. Similarly, the porous polymercoating may increase the adhesiveness of a substrate by about 1%, 2%,3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%,55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%,200%, 250%, 300% or more. In some embodiments, the porous polymercoating imparts one or more acoustic properties to and/or modulates oneor more acoustic properties of the substrate(s). For example, the porouspolymer coating may lower the air permeability of a substrate by about1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%,45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or more. Likewise,the porous polymer coating may increase the airflow resistance of asubstrate by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%,25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%,95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% or more. In someembodiments, the porous polymer coating modulates the strength of thesubstrate(s). For example, the porous polymer coating may increase thestrength of the substrate(s) by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%,9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% ormore. In some embodiments, the porous polymer coating modulates thedurability of the substrate(s). For example, the porous polymer coatingmay increase the durability of the substrate(s) by about 1%, 2%, 3%, 4%,5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%,60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%,250%, 300% or more. In some embodiments, the porous polymer coatingmodulates the abrasion resistance of the substrate(s). For example, theporous polymer coating may increase the abrasion resistance of thesubstrate(s) 6%, 7%, 8%, 9%, by about 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%,25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%,95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% or more.

As indicated above, composite materials of the present invention maycomprise any suitable combination of porous polymer coating(s) andsubstrate(s) and may be formed using any suitable technique.

Composite materials of the present invention may have any suitable basisweight. In some embodiments, composite materials of the presentinvention have a basis weight of about 10, 15, 20, 25, 30, 25, 40, 45,50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150,160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290,300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 420, 440, 460,480, 500, 520, 540, 560, 580, 600, 650, 700, 750, 800, 850, 900, 950,1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000 gsm orless. In some embodiments, composite materials of the present inventionhave a basis weight of about 10, 15, 20, 25, 30, 25, 40, 45, 50, 55, 60,65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180,190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320,330, 340, 350, 360, 370, 380, 390, 400, 420, 440, 460, 480, 500, 520,540, 560, 580, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1100, 1200,1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000 gsm or more.

Composite materials of the present invention may demonstrate reduced airpermeability. In some embodiments, the air permeability of the compositematerial is reduced by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, 96%. 97%, 98%, 99% or 100% as compared to a controlsubstrate (i.e., a substrate that lacks the porous polymer coating butis otherwise identical to the composite material) when tested based onASTM Standard C522-03, “Standard Test Method for Airflow Resistance ofAcoustical Materials,” ASTM International (2009); ASTM Standard D737-04,““Standard Test Method for Air Permeability of Textile Fabrics,” ASTMInternational (2012). In some embodiments, the substrate is a fabric(e.g., a nonwoven fabric), and the air permeability of the compositematerial is reduced by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, 96%. 97%, 98%, 99% or 100% as compared to a controlfabric having the same amounts/types of fibers, weight, thickness as thefabric of the composite material.

Composite materials of the present invention may demonstrate enhancedairflow resistance. In some embodiments, the airflow resistance of thecomposite material is increased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%,9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% ormore as compared to a control substrate (i.e., a substrate that lacksthe porous polymer coating but is otherwise identical to the compositematerial) when tested based on ASTM Standard C522-03, “Standard TestMethod for Airflow Resistance of Acoustical Materials,” ASTMInternational (2009); ASTM Standard D737-04, ““Standard Test Method forAir Permeability of Textile Fabrics,” ASTM International (2012). In someembodiments, the substrate is a fabric (e.g., a nonwoven fabric), andthe airflow resistance of the composite material is increased by about1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%,45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%,175%, 200%, 250%, 300% or more as compared to a control fabric havingthe same amounts/types of fibers, weight, thickness as the fabric of thecomposite material.

Composite materials of the present invention may have an airflowresistance of about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550,600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200,1250, 1300, 1350, 1400, 1450, 1500, 1600, 1700, 1800, 1900, 2000, 2100,2200, 2300, 2400, 2500, 2600, 2700, 2800, 2900, 3000, 3200, 3400, 3600,3800, 4000, 4200, 4400, 4600, 4800, 5000, 5500, 6000, 6500, 7000, 7500,8000, 8500, 9000, 9500, 10000 Rayls or more when based on ASTM StandardC522-03, “Standard Test Method for Airflow Resistance of AcousticalMaterials,” ASTM International (2009); ASTM Standard D737-04, ““StandardTest Method for Air Permeability of Textile Fabrics,” ASTM International(2012). In some embodiments, the composite material has an airflowresistance of about 100 to about 10,000 Rayls. In some embodiments, thecomposite material comprises, consists essentially of or consists of onesubstrate and one porous polymer coating and has an airflow resistanceof about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650,700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300,1350, 1400, 1450, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300,2400, 2500, 2600, 2700, 2800, 2900, 3000, 3200, 3400, 3600, 3800, 4000,4200, 4400, 4600, 4800, 5000, 5500, 6000, 6500, 7000, 7500, 8000, 8500,9000, 9500, 10000 Rayls or more. In some embodiments, the compositematerial comprises, consists essentially of or consists of one substrateand one porous polymer coating and has an airflow resistance of about100 to about 10,000 Rayls. In some embodiments, the composite materialcomprises, consists essentially of or consists of a porous polymercoating interposed between two substrates and has an airflow resistanceof about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650,700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300,1350, 1400, 1450, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300,2400, 2500, 2600, 2700, 2800, 2900, 3000, 3200, 3400, 3600, 3800, 4000,4200, 4400, 4600, 4800, 5000, 5500, 6000, 6500, 7000, 7500, 8000, 8500,9000, 9500, 10000 Rayls or more. In some embodiments, the compositematerial comprises, consists essentially of or consists of a porouspolymer coating interposed between two substrates and has an airflowresistance of about 100 to about 10,000 Rayls.

Composite materials of the present invention may demonstrate enhancedstrength. In some embodiments, the strength of the composite material isincreased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%,25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%,95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% or more as compared to acontrol material (i.e., a substrate that lacks the porous polymercoating but is otherwise identical to the composite material) whentested in based on ASTM Standard D1682-64, “Standard Test Methods forBreaking Load and Elongation of Textile Fabrics,” ASTM International(1975); ASTM Standard D5034-09, “Standard Test Methods for Breaking Loadand Elongation of Textile Fabrics (Grab Test),” ASTM International(2013); ASTM Standard D5035-11, “Standard Test Methods for Breaking Loadand Elongation of Textile Fabrics (Strip Method),” ASTM International(2011); ASTM Standard D1117-01, “Standard Guide for Evaluating NonwovenFabrics,” ASTM International (2001). In some embodiments, the substrateis a fabric (e.g., a nonwoven fabric), and the strength of the compositematerial is increased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% or more ascompared to a control fabric having the same amounts/types of fibers,weight, thickness as the fabric of the composite material.

Composite materials of the present invention may demonstrate enhanceddurability. In some embodiments, the durability of the compositematerial is increased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% or more ascompared to a control material (i.e., a substrate that lacks the porouspolymer coating but is otherwise identical to the composite material)when based on ASTM Standard D4157-13, “Standard Test Method for AbrasionResistance of Textile Fabrics (Oscillatory Cylinder Method),” ASTMInternational (2013); ASTM Standard D4158-08, “Standard Guide forAbrasion Resistance of Textile Fabrics (Uniform Abrasion),” ASTMInternational (2012); ASTM Standard D3389-10, ““Standard Test Method forCoated Fabrics Abrasion Resistance,” ASTM International (2010); ASTMStandard D3885-07a, “Standard Test Method for Abrasion Resistance ofTextile Fabrics (Flexing and Abrasion Method),” ASTM International(2011); ASTM Standard D3886-99, “Standard Test Method for AbrasionResistance of Textile Fabrics (Inflated Diaphragm Apparatus),” ASTMInternational (2011); ASTM Standard D4966-12, “Standard Test Method forAbrasion Resistance of Textile Fabrics (Martindale Abrasion TesterMethod),” ASTM International (2013); ASTM Standard D3884-09, “StandardTest Method for Abrasion Resistance of Textile Fabrics (Rotary Platform,Double-Head Method),” ASTM International (2013); ASTM Standard D3597-02,“Standard Specification for Woven Upholstery Fabrics-Plain, Tufted orFlocked,” ASTM International (2009); ASTM Standard D4037-02, ““StandardPerformance Specification for Woven, Knitted or Flocked BedspreadFabrics,” ASTM International (2008); ASTM Standard D1117-01, “StandardGuide for Evaluating Nonwoven Fabrics,” ASTM International (2001). Insome embodiments, the substrate is a fabric (e.g., a nonwoven fabric),and the durability of the composite material is increased by about 1%,2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%,50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%,175%, 200%, 250%, 300% or more as compared to a control fabric havingthe same amounts/types of fibers, weight, thickness as the fabric of thecomposite material.

Composite materials of the present invention may demonstrate enhancedabrasion resistance. In some embodiments, the abrasion resistance of thecomposite material is increased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%,9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% ormore as compared to a control material (i.e., a substrate that lacks theporous polymer coating but is otherwise identical to the compositematerial) when tested based on ASTM Standard D4157-13, “Standard TestMethod for Abrasion Resistance of Textile Fabrics (Oscillatory CylinderMethod),” ASTM International (2013); ASTM Standard D4158-08, “StandardGuide for Abrasion Resistance of Textile Fabrics (Uniform Abrasion),”ASTM International (2012); ASTM Standard D3389-10, ““Standard TestMethod for Coated Fabrics Abrasion Resistance,” ASTM International(2010); ASTM Standard D3885-07a, “Standard Test Method for AbrasionResistance of Textile Fabrics (Flexing and Abrasion Method),” ASTMInternational (2011); ASTM Standard D3886-99, “Standard Test Method forAbrasion Resistance of Textile Fabrics (Inflated Diaphragm Apparatus),”ASTM International (2011); ASTM Standard D4966-12, “Standard Test Methodfor Abrasion Resistance of Textile Fabrics (Martindale Abrasion TesterMethod),” ASTM International (2013); ASTM Standard D3884-09, “StandardTest Method for Abrasion Resistance of Textile Fabrics (Rotary Platform,Double-Head Method),” ASTM International (2013); ASTM Standard D3597-02,“Standard Specification for Woven Upholstery Fabrics-Plain, Tufted orFlocked,” ASTM International (2009); ASTM Standard D4037-02, ““StandardPerformance Specification for Woven, Knitted or Flocked BedspreadFabrics,” ASTM International (2008); ASTM Standard D1117-01, “StandardGuide for Evaluating Nonwoven Fabrics,” ASTM International (2001). Insome embodiments, the substrate is a fabric (e.g., a nonwoven fabric),and the abrasion resistance of the composite material is increased byabout 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%,40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%,150%, 175%, 200%, 250%, 300% or more as compared to a control fabrichaving the same amounts/types of fibers, weight, thickness as the fabricof the composite material.

Composite materials of the present invention may demonstrate enhancedadhesive properties. In some embodiments, the adhesiveness of thecomposite material is increased by about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%,9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%, 175%, 200%, 250%, 300% ormore as compared to a control material (i.e., a substrate that lacks theporous polymer coating but is otherwise identical to the compositematerial) when tested based on AATTC Standard 136, “Bond Strength ofBonded and Laminated Fabrics,” American Association of Textile Chemistsand Colorists, (2012); ASTM Standard D6862-11, “Standard Test Method for90 Degree Peel Resistance of Adhesives,” ASTM International (2012); ASTMStandard D3167-10, “Standard Test Method for Floating Roller PeelResistance of Adhesives,” ASTM International (2010); ASTM StandardD2724-07, “Standard Test Methods for Bonded, Fused, and LaminatedApparel Fabrics,” ASTM International (2011); H N Standard 0192, “TestMethod for Determining Bond Strength of Laminated Fabrics,” (2007). Insome embodiments, the substrate is a fabric (e.g., a nonwoven fabric),and the adhesiveness of the composite material is increased by about 1%,2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%,50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 125%, 150%,175%, 200%, 250%, 300% or more as compared to a control fabric havingthe same amounts/types of fibers, weight, thickness as the fabric of thecomposite material.

In addition, the porous polymer coating of the invention, may be coatedon both the top and bottom side of the substrate, which increases theeffectiveness of the product. The coated on both sides material, maythen be used on top or bottom of a sound absorbing panel, or insertedbetween two batts, foams, panels, or fabrics to improve, the acousticperformance, the sound absorption ability, or the ability to absorbcertain frequencies of sound, by the final product and allow forthermally activated adhesive bonding of the layers. Alternately theporous polymer coating of the invention, with both top and bottom coatedonto a substrate, may be inserted between dissimilar materials, such asbatts, foams, panels, fabrics, or carpet, and allow for thermallyactivated adhesive bonding of the layers.

Accordingly, composite materials of the present invention may besuitable for use in numerous applications and products, including, butnot limited to, transportation applications, building applications,architectural applications, automobiles, aircraft, air ducts,appliances, baffles, ceiling tiles and office partitions.

EXAMPLES

The following examples are not intended to be a detailed catalogue ofall the different ways in which the present invention may be implementedor of all the features that may be added to the present invention. Thoseskilled in the art will appreciate that numerous variations andadditions to the various embodiments may be made without departing fromthe present invention. Hence, the following descriptions are intended toillustrate some particular embodiments of the invention, and not toexhaustively specify all permutations, combinations and variationsthereof.

Example 1

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 3.3. The foam was coated onto a spunbond webcomprising polyester (100% by weight) with a nominal basis weight ofabout 34 gsm using a knife gap of about 40 mils. The coated web wasdried in a forced air oven for about 1 minute at approximately 155° C.The dry add-on weight of the porous polymer coating was around 93 gsm.The air permeability of the web prior to application/drying of theporous polymer coating was about 711 cfm. The air permeability of thecomposite material was about 1 cfm.

Example 2

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of 5.6. The foam was coated onto a spunbond web comprisingpolyester (100% by weight) and weighing 34 gsm using a knife gap of 40mils. The coated web was dried in a forced air oven for 1 minute at 175°C. The dry add-on weight of the porous polymer coating was approximately46.3 gsm. The air permeability of the web prior to application/drying ofthe porous polymer coating was about 711 cfm. The air permeability ofthe composite material was about 74.4 cfm.

FIG. 7 provides an exemplary image of the porous polymer coating thatwas added to the polyester spunbond web.

Example 3

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of 5.6. The foam was coated onto a spunbond web comprisingpolyester (100% by weight) with a nominal basis weight of about 34 gsmusing a knife gap of 40 mils. The coated web was dried in a forced airoven for 1 minute at 155° C. The dry add-on weight of the porous polymercoating was around 43.6 gsm. The air permeability of the web prior toapplication/drying of the porous polymer coating was about 711 cfm. Theair permeability of the composite material was about 81.8 cfm.

Example 4

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 5.6. The foam was coated onto a spunbond webcomprising polyester (100% by weight) with a nominal basis weight ofabout 34 gsm using a knife gap of about 40 mils. The coated web wasdried in a forced air oven for about 1 minute at around 175° C. The dryadd-on weight of the porous polymer coating was around 46.3 gsm.

A 12 inch by 12 inch sample of the composite material was bonded to a 12inch by 12 inch piece of corrugated kraft cardboard at around 410° F.for about 1 minute using a Tetrahedron press set at 10 tons of pressureand using 135 mil thick shims to control the amount of compressionexperienced by the composite material (the corrugated kraft cardboardwas about 165 mils thick).

After cooling, the cardboard was pulled away from the compositematerial. A significant portion of the outer facing of the corrugatedkraft cardboard remained bonded to the composite material, indicatingthat the porous polymer coating imparted excellent adhesive propertiesto the spunbond polyester web.

Example 5

A porous polymer coating was formed by introducing a mixture comprisinga blend of low T_(g) and high T_(g) acrylic binders (−15° F. and +30°F., respectively), APP, thermosetting adhesive powder, foaming agents,and thickeners into a CFS® foam generator system (Gaston Systems, Inc.,Stanley, N.C.) and foaming the mixture using air at around 80 pounds persquare inch (psi) and a blow ratio of 4. The foam was coated onto fivesamples of black, flame-retardant, water-repellant spunlaced fabriccomprising rayon about (50% by weight) and polyester about (50% byweight) and weighing on average 91 gsm, using a parabolic foamapplicator with a 0.030″ gap that was setup between the pins of a pilotline tenter frame. The coated fabric samples were dried in a forced airoven at about 150° C. for a period of time ranging from about 30 secondsto about 1 minute. Drying times were varied to allow for changes inadd-on of the coating. The air permeability of the fabric samples priorto application/drying of the porous polymer coating was on average about213 cfm.

The dry add-on weights of the porous polymer coatings and the airpermeabilities of the resultant composite materials are shown in Table 2and in FIG. 9.

TABLE 2 Characteristics of the composite materials described in Example5. Sample Dry Add-On Weight (osy) Avg. Air Perm (cfm) Control (uncoated)0.0 213 1 0.4 75 2 0.5 64 3 0.7 50 4 0.8 39 5 1.0 31

Example 6

A porous polymer coating was formed by introducing UNIBOND 2780B(Unichem, Inc., Haw River, N.C.) into a CFS® foam generator system(Gaston Systems, Inc., Stanley, N.C.) and foaming the mixture using airat around 80 pounds per square inch (psi) and a blow ratio of 4. Thefoam was coated onto seven samples of black, flame-retardant,water-repellant spunlaced fabric comprising woodpulp (about 55% byweight) and polyester (about 45% by weight) and weighing on averageabout 72 gsm using a parabolic foam applicator with a 0.020″ gap thatwas setup between the pins of a pilot line tenter frame. The coatedfabric samples were dried in a forced air oven at about 150° C. for aperiod of time ranging from about 30 seconds to about 1 minute. The airpermeability of the fabric samples prior to application/drying of theporous polymer coating was on average about 66 cfm.

The dry add-on weights of the porous polymer coatings and the airpermeabilities of the resultant composite materials are shown in Table 3and in FIG. 10.

TABLE 3 Characteristics of the composite materials described in Example6. Sample Dry Add-On Weight (osy) Avg. Air Perm (cfm) Control (uncoated)0.0 66 1 0.45 23 2 0.5 21 3 0.6 18 4 0.65 13 5 0.79 9 6 0.9 5 7 1.1 4

Example 7

A porous polymer coating was formed by introducing UNIBOND 2780B(Unichem, Inc., Haw River, N.C.) into a CFS® foam generator system(Gaston Systems, Inc., Stanley, N.C.) and foaming the mixture using airat around 80 pounds per square inch (psi) and a blow ratio of 4. Thefoam was coated onto a black, flame-retardant, water-repellant spunlacedfabric comprising woodpulp (about 55% by weight) and polyester (about45% by weight) and weighing on average about 72 gsm using a segmentedfoam applicator and a tenter frame. The coated fabric samples were driedin a forced air oven for about 30 seconds at about 275° F. The dryadd-on weight of the porous polymer coating was on average about 0.8ounces per square yard (osy). The air permeability of the fabric sampleprior to application/drying of the porous polymer coating was on averageabout 66 cfm. The air permeability of the composite material was onaverage about 30 cfm.

Example 8

A porous polymer coating was formed by introducing UNIBOND 2780B(Unichem, Inc., flaw River, N.C.) into a CFS® foam generator system(Gaston Systems, Inc., Stanley, N.C.) and foaming the mixture usingpressurized air at around 80 pounds per square inch (psi) and a blowratio of 4. The foam was coated onto a black, flame-retardant,water-repellant spunlaced fabric comprising woodpulp (about 55% byweight) and polyester (about 45% by weight) and weighing on averageabout 72 gsm using a segmented foam applicator and a tenter frame. Thecoated fabric samples were dried in a forced air oven for about 30seconds at about 300° F. The dry add-on weight of the porous polymercoating was approximately 0.8 ounces per square yard (osy). The airpermeability of the fabric sample prior to application/drying of theporous polymer coating was on average about 66 cfm. The air permeabilityof the composite material was on average about 19 cfm.

Example 9

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of around 10.4. The foam was coated onto aspunbond/meltblown/spunbond web comprising polypropylene (100% byweight) with a nominal basis weight around 44 gsm using a knife gap ofabout 40 mils. The coated web was dried in a forced air oven for 1minute at 140° C. The dry add-on weight of the porous polymer coatingwas about 14.1 gsm. The air permeability of the web (prior toapplication/drying of the porous polymer coating was about 40 cfm. Theair permeability of the composite material was about 28.3 cfm.

FIG. 8 provides an exemplary image of the porous polymer coating thatwas added to the polypropylene spunbond/meltblown/spunbond web.

The composite material was bonded to a 0.8 inch thick, 430 gsm nonwovenbatt comprising polyester (about 80% to about 99% by weight) and a lowermelt polymer (about 1% to about 20% by weight) (Vita Nonwovens, LLC,High Point, N.C.) as outlined below:

-   -   A Despatch LBB/LED Series 2400 Watt, 20 amp convection oven        (Despatch Industries, Minneapolis, Minn.), which is capable of        heating to a temperature of 200-400° F. and of maintaining a        temperature within ±3° F. of a target temperature, was preheated        to 193° F.    -   A 12 inch by 12 inch aluminum plate weighing 1600 grams was        placed in the oven and allowed to stabilize to 193±3° F. The        temperature of the aluminum plate was confirmed using a contact        thermocouple (measuring the temperature of the middle of the        plate and of each corner of the plate).    -   A 12 inch by 12 inch sample of the composite material was placed        on the bench top with the porous polymer coating facing up.    -   The composite material sample was overlaid with a 12 inch by 12        inch piece of the nonwoven batt (ensuring that the edges of the        composite material and the batt were aligned).    -   The composite-batt stack was placed in the oven atop the        preheated aluminum plate with the nonwoven batt facing up        (ensuring that the edges of the preheated aluminum plate and the        composite-batt stack were aligned).    -   After 15 seconds, a 12 inch by 12 inch aluminum plate weighing        2400-2500 grams was placed in the oven atop the preheated        aluminum plate and the composite-batt stack (ensuring that the        edges of the aluminum plates and the composite-batt stack were        aligned).    -   After 45 seconds, the top plate was removed and the        composite-batt stack was removed from the oven and placed on the        bench top to cool for 5 minutes.

The bond between the porous polymeric layer of the composite materialand the nonwoven batt had an average peel strength of over 100grams/inch when tested based on ASTM D903-98. (“Standard Test Method forPeel or Stripping Strength of Adhesive Bonds,” ASTM International(2010)),

Example 10

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 3 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 4.3. The foam was coated onto samples of aspunbond web comprising polyester (100% by weight) with a nominal basisweight of about 34 gsm using a rounded coating blade and a gap of about15, 22 or 29 mils. The coated web was dried in a forced air oven forabout 1 minute at approximately 155° C. When tested based on ASTMStandard D3776-09 (“Standard Test Methods for Mass per Unit Area(Weight) of Fabric,” ASTM International (2013)), the dry add-on weightsof the porous polymer coatings were around 1.40, 1.98 and 2.61 osy,respectively. The air permeability of the sampled web prior toapplication/drying of the porous polymer coating averaged about 711 cfm.When tested based on ASTM Standard D737-96 (“Standard Test Method forAir Permeability of Textile Fabrics,” ASTM International (1996)), theair permeabilities of the composite materials were approximately 113, 52and 15 cfm, respectively.

The dry add-on weights of the porous polymer coatings and the airpermeabilities of the resultant composite materials are shown in Table 4and in FIG. 11 (diamonds).

TABLE 4 Characteristics of the composite materials described in Example10. Coating Gap (mil) Dry Add-On Weight (osy) Avg. Air Perm. (cfm) 151.4 113.0 22 1.98 52.4 29 2.61 15.6

Example 11

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 4 of Table 1 above into a CFSfoam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 5. The foam was coated onto samples of aspunbond web comprising polyester (100% by weight) with a nominal basisweight of about 34 gsm using a rounded coating blade and a gap of about15, 22 or 29 mils. The coated web was dried in a forced air oven forabout 1 minute at approximately 155° C. When tested based on ASTMStandard D3776-09 (“Standard Test Methods for Mass per Unit Area(Weight) of Fabric,” ASTM International (2013)), the dry add-on weightsof the porous polymer coatings were around 0.56, 0.74 and 0.90 osy,respectively. The air permeability of the sampled web prior toapplication/drying of the porous polymer coating averaged about 711 cfm.When tested based on ASTM Standard D737-96 (“Standard Test Method forAir Permeability of Textile Fabrics,” ASTM International (1996)), theair permeabilities of the composite materials were approximately 279,155 and 39 cfm, respectively.

The dry add-on weights of the porous polymer coatings and the airpermeabilities of the resultant composite materials are shown in Table 5and in FIG. 11 (squares).

TABLE 5 Characteristics of the composite materials described in Example11. Coating Gap (mil) Dry Add-On Weight (osy) Avg. Air Perm. (cfm) 150.56 279.7 22 0.74 155.5 29 0.90 39.2

Example 12

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 3 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 4.3. The foam was coated onto samples of aspunbond web comprising polyester (100% by weight) with a nominal basisweight of about 34 gsm using a rounded coating blade and a gap of about15, 22 or 29 mils. The coated web was dried in a forced air oven forabout 1 minute at approximately 155° C. When tested based on ASTMStandard D3776-09 (“Standard Test Methods for Mass per Unit Area(Weight) of Fabric,” ASTM International (2013)), the dry add-on weightsof the porous polymer coatings were approximately 1.40, 1.98 and 2.61osy, respectively. The air permeability of the sampled web prior toapplication/drying of the porous polymer coating averaged about 711 cfm.When tested based on ASTM Standard D737-96 (“Standard Test Method forAir Permeability of Textile Fabrics,” ASTM International (1996)), theair permeabilities of the composite materials were reduced byapproximately 556, 616 and 653 cfm, respectively.

The dry add-on weights of the porous polymer coatings and the airpermeability reductions and air permeability reduction efficiencies ofthe resultant composite materials are shown in Table 6.

TABLE 6 Characteristics of the composite materials described in Example12. Avg. Air Coating Dry Add-On Avg. Air Perm. Perm. Reduction Gap (mil)Weight (osy) Reduction (cfm) Efficiency (cfm/osy) 15 1.4 556.0 397.72 221.98 616.6 311.72 29 2.61 653.4 250.75

Example 13

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 4 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 5. The foam was coated onto samples of aspunbond web comprising polyester (100% by weight) with a nominal basisweight of about 34 gsm using a rounded coating blade and a gap of about15, 22 or 29 mils. The coated web was dried in a forced air oven forabout 1 minute at approximately 155° C. When tested based on ASTMStandard D3776-09 (“Standard Test Methods for Mass per Unit Area(Weight) of Fabric,” ASTM International (2013)), the dry add-on weightsof the porous polymer coatings were around 1.40, 1.98 and 2.61 osy,respectively. The air permeability of the sampled web prior toapplication/drying of the porous polymer coating averaged about 711 cfm.When tested based on ASTM Standard D737-96 (“Standard Test Method forAir Permeability of Textile Fabrics,” ASTM International (1996)), theair permeabilities of the composite materials were reduced by 389.3,513.5 and 629.8 cfm, respectively.

The dry add-on weights of the porous polymer coatings and the airpermeability reductions and air permeability reduction efficiencies ofthe resultant composite materials are shown in Table 7.

TABLE 7 Characteristics of the composite materials described in Example13. Avg. Air Coating Dry Add-On Avg. Air Perm Perm. Reduction Gap (mil)Weight (osy) Reduction (cfm) Efficiency (cfm) 15 0.56 389.3 697.77 220.74 513.5 692.25 29 0.90 629.8 699.56

Example 14

A porous polymer coating was formed by introducing a mixture accordingto Formula 1 of Table 1 above into a CFS® foam generator system (GastonSystems, Inc., Stanley, N.C.) and foaming the mixture using air ataround 80 pounds per square inch (psi) and a blow ratio of approximately4.3. The foam was coated onto samples of a spunbond web comprisingpolyester (100% by weight) and weighing 34 gsm using a rounded coatingblade and a gap of about 15, 22 or 29 mils. The coated web was dried ina forced air oven for about 1 minute at approximately 155° C. Whentested based on ASTM Standard D3776-09 (“Standard Test Methods for Massper Unit Area (Weight) of Fabric,” ASTM International (2013)), the dryadd-on weights of the porous polymer coatings were around 1.40, 1.98 and2.61 osy, respectively.

The dry add-on weights of the porous polymer coatings are shown in Table8 and in FIG. 12 (squares).

TABLE 8 Characteristics of the composite materials described in Example14. Coating Gap (mil) Dry Add-On Weight (osy) 15 1.40 22 1.98 29 2.61

A 12 inch by 12 inch sample of the composite material was bonded to a 12inch by 12 inch piece of corrugated kraft cardboard at 430° F. for inminute using 5 tons of pressure and 135 mil thick shims to control theamount of compression experienced by the composite material (thecorrugated kraft cardboard was about 165 mils thick). This was doneusing a Tetrahedron press, model number 1301 (from TetrahedronAssociates, Inc., San Diego, Calif.) according to the manufacturer'sinstructions.

After cooling, the cardboard was pulled away from the compositematerial. A significant portion of the outer facing of the corrugatedkraft cardboard remained bonded to the composite material, indicatingthat the porous polymer coating imparted excellent adhesive propertiesto the spunbond polyester web.

Example 15

A porous polymer coating was formed by introducing a styrene acryliccopolymer mixture according to Formula 2 of Table 1 above into a CFS®foam generator system (Gaston Systems, Inc., Stanley, N.C.) and foamingthe mixture using air at around 80 pounds per square inch (psi) and ablow ratio of approximately 3.3. The foam was coated onto samples of aspunbond web comprising polyester (100% by weight) with a nominal basisweight of about 34 gsm using a rounded coating blade and a gap of about15, 22 or 29 mils. The coated web was dried in a forced air oven forabout 1 minute at approximately 155° C. When tested based on ASTMStandard D3776-09 (“Standard Test Methods for Mass per Unit Area(Weight) of Fabric,” ASTM International (2013)), the dry add-on weightsof the porous polymer coatings were around 0.56, 0.74 and 0.90 osy,respectively.

The dry add-on weights of the porous polymer coatings are shown in Table9 and in FIG. 12 (triangles).

TABLE 9 Characteristics of the composite materials described in Example15. Coating Gap (mil) Dry Add-On Weight (osy) 15 0.56 22 0.74 29 0.90

A 12 inch by 12 inch sample of the composite material was bonded to a 12inch by 12 inch piece of corrugated kraft cardboard at 410° F. for inminute using 10 tons of pressure and 135 mil thick shims to control theamount of compression experienced by the composite material (thecorrugated kraft cardboard was about 165 mils thick).

After cooling, the cardboard was pulled away from the compositematerial. A significant portion of the outer facing of the corrugatedkraft cardboard remained bonded to the composite material, indicatingthat the porous polymer coating imparted excellent adhesive propertiesto the spunbond polyester web.

The foregoing is illustrative of the present invention and is not to beconstrued as limiting thereof. Although a few exemplary embodiments ofthis invention have been described, those skilled in the art willreadily appreciate that many modifications are possible in the exemplaryembodiments without materially departing from the novel teachings andadvantages of this invention. Accordingly, all such modifications areintended to be included within the scope of this invention as defined inthe claims. The invention is defined by the following claims, withequivalents of the claims to be included therein.

1. A porous polymer coating comprising: a polymeric foam havingthermally activated adhesive properties, a void fraction of greater thanabout 15%, and an air permeability greater than 1 cubic feet per minuteper square foot as measured based on ASTM D737-04, wherein saidpolymeric foam comprises a plurality of open cells; wherein saidpolymeric foam comprises an acrylic binder; and wherein said porouspolymer coating has an airflow resistance in a range of about 200 Raylsto about 10,000 Rayls as measured based on ASTM C522-03.
 2. The porouspolymer coating of claim 1, wherein said polymeric foam furthercomprises at least one thermoplastic polymer and the at least oneadditional thermoplastic polymer is selected from the group consistingof: polyacrylates, polyvinylacetates, styrene butadiene rubbers,diallylorthophthalates, ionomers, formulated epoxys, polysulfones,polyether-etherketones, acrylonitrilebutadienstyrenes, polycarbonates,vinylesters, styrene copolymers, polyamides, polyamines,ethylenevinylacetates, polyvinylalcohols, polyvinylchlorides,polyvinylidiene chloride, chlorinated polyethylenes, polyesters,nitriles, and polyethylenes.
 3. The porous polymer coating of claim 1,wherein said polymeric foam comprises one or more non-thermoplasticpolymers. 4-6. (canceled)
 7. The porous polymer coating of claim 1,wherein said airflow resistance greater than about 250 Rayls as measuredbased on ASTM C522-03.
 8. The porous polymer coating of claim 1, whereinsaid airflow resistance is in a range of about 500 Rayls to about 2,500Rayls as measured based on ASTM C522-03.
 9. The porous polymer coatingof claim 1, wherein said airflow resistance is greater than about 1000Rayls as measured based on ASTM C522-03.
 10. The porous polymer coatingof claim 1, wherein said airflow resistance is in a range of about 500Rayls to about 2,500 Rayls as measured based on ASTM C522-03.
 11. Theporous polymer coating of claim 1, wherein said air permeability isgreater than about 10 cubic feet per minute per square foot as measuredbased on ASTM D737-04.
 12. The porous polymer coating of claim 1,wherein said air permeability is greater than about 40 cubic feet perminute per square foot as measured based on ASTM D737-04.
 13. The porouspolymer coating of claim 1, wherein said air permeability is greaterthan about 73 cubic feet per minute per square foot as measured based onASTM D737-04.
 14. The porous polymer coating of claim 1, wherein saidporous polymer coating has a basis weight of about 10 grams per squaremeter to about 75 grams per square meter.
 15. The porous polymer coatingof claim 1, wherein said porous polymer coating has a basis weight ofabout 10 grams per square meter to about 45 grams per square meter. 16.The porous polymer coating of claim 1, wherein the polymeric foam is areticulated polymeric foam.
 17. The porous polymer coating of claim 1,further comprising thermally activatable adhesive particles.
 18. Theporous polymer coating of claim 1, further comprising a filled latexpolymer coating.
 19. The porous polymer coating of claim 1, furthercomprising an additive containing latex polymer coating.
 20. A compositematerial, comprising: a first substrate; a second substrate; and theporous polymer coating of claim 1 interposed between said firstsubstrate and second substrate. 21-31. (canceled)
 32. A method offorming a composite material, comprising: applying the porous polymercoating of claim 1 to a substrate. 33-42. (canceled)
 43. The porouspolymer coating of claim 1, wherein said air permeability is in a rangeof about 5 cfm/sq. ft. to about 100 cfm/sq. ft. as measured based onASTM D737-04.
 44. The porous polymer coating of claim 1, wherein thevoid fraction is in a range of about 20% to about 50%.